#iso14971

The interrelationship between EN ISO 14971:2019/A11:2021 and the General Safety and Performance Requirements of Regulation holds great significance for device manufacturers in the EU. Collaborating with regulatory experts and notified bodies can further aid manufacturers in traversing these requirements adeptly and achieving compliance with plan.

https://www.medikalkalite.com/iso-14971-ve-risk-yonetimi/

This comprehensive white paper can be helpful for medical device companies to strategically update their risk management process to not only satisfy the ISO 14971 standard, but to improve their risk management process.

Get Register your medicinal product for the international market. 

#DesignandDevelopment of the product plays a vital role in the total life cycle of a product and to ensure the effective and safe product in the market.  #DesignVerification